Canonical Allele Identifier: CA14031369

Gene: SLC35F4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.57888330A>G , CM000676.2:g.57888330A>G	GRCh38
NC_000014.8:g.58355048A>G , CM000676.1:g.58355048A>G	GRCh37
NC_000014.7:g.57424801A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556568.1:n.282+93583T>C
XM_011536723.1:c.64+93583T>C	XP_011535025.1:n.64+93583T>C
XM_011536723.3:c.64+93583T>C	XP_011535025.1:n.64+93583T>C